Literature DB >> 20006508

Morphometry of the thoracolumbar vertebrae in sickle cell disease.

Yurdal Serarslan1, Aydiner Kalaci, Cenk Ozkan, Yunus Doğramaci, Cengiz Cokluk, Ahmet Nedim Yanat.   

Abstract

Patients with sickle cell disease (SCD) who have deformities and vertebral fractures due to osteoporosis may require surgery. Spinal surgeons must become familiar with the vertebral morphometry of patients with SCD and to that aim we have examined the morphometry of the thoracolumbar spine in these patients. A cohort of 100 patients with SCD was examined using plain thoraco lumbar anteroposterior/lateral radiographs and dual energy X-ray absorptiometry (DEXA). Vertebral morphometry (vertebral body diameters, pedicle, spinal canal and deformity) was assessed for different age groups. Results were compared to published studies of healthy subjects. The vertebral dimensions for the 16-20-year and the 21+-year-old groups were significantly smaller for females than males at most spinal levels, while measurements in the 6-10 years and 11-15 years age groups were similar across both sexes at most levels. No significant statistical difference was found between the diameters of the right and left pedicles. With the exception of the sagittal diameter, most of the dimensions of the vertebral bodies measured in SCD patients were less than those of healthy individuals; multiple deformities were also observed. Low bone density was noted in 32 patients. Our data highlight the differences in vertebral bone mineral density, anatomy and deformities in patients with SCD compared to healthy individuals. When considering surgical intervention for patients with SCD, it is important that pre-operative radiography and planning is undertaken, and that the surgeon is familiar with the geometry of the pedicles of the thoracolumbar vertebrae necessary for the safe insertion of pedicle screws. Osteoporosis must be considered when planning surgical interventions in these patients. Copyright 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 20006508     DOI: 10.1016/j.jocn.2009.05.010

Source DB:  PubMed          Journal:  J Clin Neurosci        ISSN: 0967-5868            Impact factor:   1.961


  7 in total

1.  Predictors of osteoclast activity in patients with sickle cell disease.

Authors:  Mehdi Nouraie; Kevin Cheng; Xiaomei Niu; Evadne Moore-King; Margaret F Fadojutimi-Akinsi; Caterina P Minniti; Craig Sable; Sohail Rana; Niti Dham; Andrew Campbell; Gregory Ensing; Gregory J Kato; Mark T Gladwin; Oswaldo L Castro; Victor R Gordeuk
Journal:  Haematologica       Date:  2011-05-05       Impact factor: 9.941

Review 2.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

3.  Status of vitamin D in children with sickle cell disease living in Madrid, Spain.

Authors:  Carmen Garrido; Elena Cela; Cristina Beléndez; Cristina Mata; Jorge Huerta
Journal:  Eur J Pediatr       Date:  2012-09-05       Impact factor: 3.183

4.  Low bone mass density is associated with hemolysis in Brazilian patients with sickle cell disease.

Authors:  Gabriel Baldanzi; Fabiola Traina; João Francisco Marques Neto; Allan Oliveira Santos; Celso Dario Ramos; Sara T Olalla Saad
Journal:  Clinics (Sao Paulo)       Date:  2011       Impact factor: 2.365

Review 5.  [Vitamin D in children and adolescents with sickle cell disease: an integrative review].

Authors:  Jacqueline Faria de Oliveira; Natália Gomes Vicente; Juliana Pereira Pontes Santos; Virgínia Resende Silva Weffort
Journal:  Rev Paul Pediatr       Date:  2015-06-10

6.  Pilot randomized controlled trial to evaluate the effect of aquatic and land physical therapy on musculoskeletal dysfunction of sickle cell disease patients.

Authors:  Camila Tatiana Zanoni; Fábio Galvão; Alberto Cliquet Junior; Sara Teresinha Olalla Saad
Journal:  Rev Bras Hematol Hemoter       Date:  2014-11-21

7.  Development of Algorithm for Clinical Management of Sickle Cell Bone Disease: Evidence for a Role of Vertebral Fractures in Patient Follow-up.

Authors:  Lucia De Franceschi; Daniele Gabbiani; Andrea Giusti; Gianluca Forni; Filippo Stefanoni; Valeria Maria Pinto; Giulia Sartori; Manuela Balocco; Chiara Dal Zotto; Maria Teresa Valenti; Luca Dalle Carbonare
Journal:  J Clin Med       Date:  2020-05-25       Impact factor: 4.241

  7 in total

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